Karzel K, Padberg D W
Arzneimittelforschung. 1977;27(3):533-8.
Murine embryonic fibroblast monolayer cultures were used to study the influence of the antirheumatic phenylacetic acid derivatives ibufanac, ibuprofen, alclofenac and bufexamac and of phenylbutazone as a reference compound on glycosaminoglycan (GAG) metabolism viability and multiplication of cells cultured in vitro. The phenylacetic acid derivatives as well as phenylbutazone showed in concentrations between 10(-3) and 10(-5) M a significant inhibitory effect on GAG production and in concentrations between 10(-3) and 3.3 X 10(-4) M a cytostatic effect; bufexamac was cytostatically active up to the concentration of 10(-5) M. Ibufenac, ibuprofen and alclofenac exhibited a similar behaviour as other non-steroidal antirheumatic drugs regarding their influence of GAG metabolism and on cell multiplication.
采用小鼠胚胎成纤维细胞单层培养法,研究抗风湿性苯乙酸衍生物异丁苯乙酸、布洛芬、氯苯酰酸和丁苯羟酸以及作为参照化合物的保泰松对体外培养细胞糖胺聚糖(GAG)代谢、活力及增殖的影响。苯乙酸衍生物以及保泰松在浓度为10⁻³至10⁻⁵M时对GAG生成具有显著抑制作用,在浓度为10⁻³至3.3×10⁻⁴M时具有细胞生长抑制作用;丁苯羟酸在浓度达10⁻⁵M时具有细胞生长抑制活性。异丁苯乙酸、布洛芬和氯苯酰酸在对GAG代谢及细胞增殖的影响方面,表现出与其他非甾体类抗风湿药物相似的特性。